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Origin of poor photovoltaic performance of bis(tetracyanoantrathiophene) non-fullerene acceptor. / Kobeleva, E. S.; Popov, A. A.; Baranov, D. S. et al.

In: Chemical Physics, Vol. 546, 111162, 01.06.2021.

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Kobeleva ES, Popov AA, Baranov DS, Uvarov MN, Nevostruev DA, Degtyarenko KM et al. Origin of poor photovoltaic performance of bis(tetracyanoantrathiophene) non-fullerene acceptor. Chemical Physics. 2021 Jun 1;546:111162. doi: 10.1016/j.chemphys.2021.111162

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Kobeleva, E. S. ; Popov, A. A. ; Baranov, D. S. et al. / Origin of poor photovoltaic performance of bis(tetracyanoantrathiophene) non-fullerene acceptor. In: Chemical Physics. 2021 ; Vol. 546.

BibTeX

@article{c69e7d065ae94f5f8e6b73445264683e,
title = "Origin of poor photovoltaic performance of bis(tetracyanoantrathiophene) non-fullerene acceptor",
abstract = "Light-induced EPR and out-of-phase electron spin echo techniques were applied to identify the origin of low photovoltaic performance of novel non-fullerene antrathiophene-based acceptor 2,2′-[2,2′-(9,9-dioctyl-9H-fluorene-2,7-diyl)bis(anthra[2,3-b]thiophene-5,10-diylidene)]tetrapropanedinitrile (AT1), compared to conventional fullerene acceptors. These techniques revealed that average trapping energy of electrons in PCDTBT/AT1 blend is higher than that in the blends of PCDTBT with fullerene acceptors, while the distance of the initial photo-induced electron transfer is decreased. These two effects are suggested to enhance the efficiency of geminate recombination in PCDTBT/AT1 blend and reduce the yield of free charges, which is supposed to be the main reason for poor OPV performance of AT1-containing blends. Low electron mobility μe = 3.5 *10-6 cm2V-1s−1 is estimated for AT1 from photo-CELIV experiment. Strong localization of the electrons on terminal acceptor units of AT1 consistently explains both efficient geminate recombination in blends of antrathiophene-based acceptor with polymer donors and low electron mobility in AT1.",
keywords = "Electron spin echo, EPR spectroscopy, Fullerenes, Mobility, Organic photovoltaics, Recombination",
author = "Kobeleva, {E. S.} and Popov, {A. A.} and Baranov, {D. S.} and Uvarov, {M. N.} and Nevostruev, {D. A.} and Degtyarenko, {K. M.} and Gadirov, {R. M.} and Sukhikh, {A. S.} and Kulik, {L. V.}",
note = "Funding Information: This work was supported by RFBR grants № 19-03-00149a and № 20-33-70126 and by state assignment to Voevodsky Institute of Chemical Kinetics and Combustion SB RAS, number AAAA-A21-121011390038-1. Publisher Copyright: {\textcopyright} 2021 Elsevier B.V. Copyright: Copyright 2021 Elsevier B.V., All rights reserved.",
year = "2021",
month = jun,
day = "1",
doi = "10.1016/j.chemphys.2021.111162",
language = "English",
volume = "546",
journal = "Chemical Physics",
issn = "0301-0104",
publisher = "Elsevier",

}

RIS

TY - JOUR

T1 - Origin of poor photovoltaic performance of bis(tetracyanoantrathiophene) non-fullerene acceptor

AU - Kobeleva, E. S.

AU - Popov, A. A.

AU - Baranov, D. S.

AU - Uvarov, M. N.

AU - Nevostruev, D. A.

AU - Degtyarenko, K. M.

AU - Gadirov, R. M.

AU - Sukhikh, A. S.

AU - Kulik, L. V.

N1 - Funding Information: This work was supported by RFBR grants № 19-03-00149a and № 20-33-70126 and by state assignment to Voevodsky Institute of Chemical Kinetics and Combustion SB RAS, number AAAA-A21-121011390038-1. Publisher Copyright: © 2021 Elsevier B.V. Copyright: Copyright 2021 Elsevier B.V., All rights reserved.

PY - 2021/6/1

Y1 - 2021/6/1

N2 - Light-induced EPR and out-of-phase electron spin echo techniques were applied to identify the origin of low photovoltaic performance of novel non-fullerene antrathiophene-based acceptor 2,2′-[2,2′-(9,9-dioctyl-9H-fluorene-2,7-diyl)bis(anthra[2,3-b]thiophene-5,10-diylidene)]tetrapropanedinitrile (AT1), compared to conventional fullerene acceptors. These techniques revealed that average trapping energy of electrons in PCDTBT/AT1 blend is higher than that in the blends of PCDTBT with fullerene acceptors, while the distance of the initial photo-induced electron transfer is decreased. These two effects are suggested to enhance the efficiency of geminate recombination in PCDTBT/AT1 blend and reduce the yield of free charges, which is supposed to be the main reason for poor OPV performance of AT1-containing blends. Low electron mobility μe = 3.5 *10-6 cm2V-1s−1 is estimated for AT1 from photo-CELIV experiment. Strong localization of the electrons on terminal acceptor units of AT1 consistently explains both efficient geminate recombination in blends of antrathiophene-based acceptor with polymer donors and low electron mobility in AT1.

AB - Light-induced EPR and out-of-phase electron spin echo techniques were applied to identify the origin of low photovoltaic performance of novel non-fullerene antrathiophene-based acceptor 2,2′-[2,2′-(9,9-dioctyl-9H-fluorene-2,7-diyl)bis(anthra[2,3-b]thiophene-5,10-diylidene)]tetrapropanedinitrile (AT1), compared to conventional fullerene acceptors. These techniques revealed that average trapping energy of electrons in PCDTBT/AT1 blend is higher than that in the blends of PCDTBT with fullerene acceptors, while the distance of the initial photo-induced electron transfer is decreased. These two effects are suggested to enhance the efficiency of geminate recombination in PCDTBT/AT1 blend and reduce the yield of free charges, which is supposed to be the main reason for poor OPV performance of AT1-containing blends. Low electron mobility μe = 3.5 *10-6 cm2V-1s−1 is estimated for AT1 from photo-CELIV experiment. Strong localization of the electrons on terminal acceptor units of AT1 consistently explains both efficient geminate recombination in blends of antrathiophene-based acceptor with polymer donors and low electron mobility in AT1.

KW - Electron spin echo

KW - EPR spectroscopy

KW - Fullerenes

KW - Mobility

KW - Organic photovoltaics

KW - Recombination

UR - http://www.scopus.com/inward/record.url?scp=85102567808&partnerID=8YFLogxK

U2 - 10.1016/j.chemphys.2021.111162

DO - 10.1016/j.chemphys.2021.111162

M3 - Article

AN - SCOPUS:85102567808

VL - 546

JO - Chemical Physics

JF - Chemical Physics

SN - 0301-0104

M1 - 111162

ER -

ID: 28090136